0571-26280011

epi@eastpoint.com.cn

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About Us
Drawing on the unique characteristics of our customers' medical device products, we offer a tailored and personalized integrated service model that spans from preclinical to clinical research and registration consultation. Our aim is to provide comprehensive support throughout the product development lifecycle, ensuring the delivery of essential preclinical research data, conducting rigorous clinical research, and facilitating seamless registration declaration processes.
Business
Drawing on the unique characteristics of our customers' medical device products, we offer a tailored and personalized integrated service model that spans from preclinical to clinical research and registration consultation. Our aim is to provide comprehensive support throughout the product development lifecycle, ensuring the delivery of essential preclinical research data, conducting rigorous clinical research, and facilitating seamless registration declaration processes.
Business Acceptance

Business Acceptance

Drawing on the unique characteristics of our customers' medical device products, we offer a tailored and personalized integrated service model that spans from preclinical to clinical research and registration consultation. Our aim is to provide comprehensive support throughout the product development lifecycle, ensuring the delivery of essential preclinical research data, conducting rigorous clinical research.
News Center
To best serve our customers' needs, we offer a personalized integrated service model tailored to the characteristics of their medical device products. This model encompasses a comprehensive range of services from preclinical to clinical research and registration consultation, ensuring the provision of essential preclinical research data, conducting robust clinical research, and facilitating seamless registration declaration processes.
Team Introduction
Based on the unique features of the customer's medical device products, we tailor a personalized integrated service model spanning from preclinical to clinical research and registration consultation. This enables us to better assist customers by providing comprehensive support, including basic preclinical research data, clinical research, and assistance with registration declaration for the product.

Training,Education,Promotion,and Academic Exchanges on Novel Medical Device

With efficient professional service capabilities, extensive senior solution experience, and a wealth of project service experience, we uphold the highest industry standards and quality requirements. Our commitment is to provide a full-cycle service chain for clinical research tailored to various product mechanisms and clinical application scenarios.

Drawing upon the unique characteristics of each product, we  plan the optimal registration solution and deliver a a full cycle service chain for product registration.

Core equipment

A clinical research and registration consulting team led by an expert level professional team

ISO 9001 Quality Certification

Integrated clinical research and product registration full cycle service chain

Strategic cooperation with leading medical device CROs in Europe

Promote work in all areas by drawing upon the experience gained on key points to expedite scientific transformation

While adhering to the core concepts of professionalism, efficiency, and innovation, and the principles of rigor and practicality, we provide full-process and new standard services for the innovative development of medical devices worldwide

Contact information: 0571-26280011